has characteristic has characteristic Juvenile onset juvenile nephropathic cystinosis https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4985 https://www.malacards.org/card/cystinosis_late_onset_juvenile_or_adolescent_nephropathic_type SCTID:22830006 NANDO:2201235 cystinosis, late-onset juvenile or adolescent nephropathic MEDGEN:75701 OMIM:219900 Orphanet:411634 icd11.foundation:422905632 MONDO:0009066 NANDO:1200163 MESH:C562683 intermediate cystinosis UMLS:C0268626 Nephropathic juvenile cystinosis is the intermediate form, in regards to severity and age of onset, of cystinosis, a metabolic disease characterized by an accumulation of cystine inside the lysosomes that causes damage in different organs and tissues, particularly in the kidneys and eyes. GARD:0017685 juvenile nephropathic cystinosis juvenile cystinosis inborn disorder of amino acid transport obsolete nephropathy secondary to a storage or other metabolic disease nephropathic cystinosis